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Renovos secures FDA breakthrough status for bone graft alternative

When injected, Renovite acts as a scaffold for cells and helps localize and retain molecules that stimulate healing

Renovos Biologics has received breakthrough designation for a synthetic nanoclay gel scaffold designed to support localized bone formation.

The Food and Drug Administration granted breakthrough status to a product, Renovite BMP-2, that Renovos sees as an alternative to bone graft materials for interbody spinal fusion.

Medtech company Biocomposites invested in Renovos last year to help fund pre-market approval in spine, trauma and orthopedics applications.

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